Objetivo The search for new drugs and antibiotics remains a very important activity. In this context, peptides continue to play a central role. There are many examples of biologically active peptides, including examples of cyclic and cyclic structures. Unlike their cyclic congeners, cyclic peptides exhibit substantial resistance to proteoloyticenzymes, and can exhibit both irreversible and reversible inhibition of such enzymes, and for this reason they are potential drugs. Some examples of natural products falling into this class include the angiotensin converting enzyme inhibitor K-13 and the amino peptidase inhibitor OF4949-III. There is therefore substantial interest in the preparation of analogues of these compounds as potential therapeutic agents. The Host group has recently completed the shortest synthesis of K-13 so far reported. This new route relies on the preparation of a highly functionalised tripe tide organizing reagent, which can be prepared efficiently from simple starting materials, and which can then be converted using palladium catalysis into the cyclic peptide. With this precedent, the objective of this project is to develop synthetic routes to the naturally occurring antibiotic biphenomycin B and the recently discovered protease inhibitors of the TMC-95 class, which are also macro cyclic peptides, together with less oxidised analogues of TMC-95. It is planned to use a similar strategy, involving the intermolecular coupling of highly functionalised organizing reagents with aryl iodides, catalysed by palladium (0). The benefit of this route is that it minimises the use of protection and deprotectionsteps, thus ensuring an efficient synthesis. The use of peptide derivatives containing two carbon-zinc bonds will also be explored, since this would allow Avery fast synthesis of biphenomycin B. Reagents such as this have never been previously prepared, and this represents a substantial element of novelty. Ámbito científico natural sciencesbiological sciencesmicrobiologybacteriologynatural scienceschemical sciencesinorganic chemistrytransition metalsnatural sciencesbiological sciencesmicrobiologymycologynatural sciencesbiological scienceszoologyentomologynatural sciencesbiological sciencesbiochemistrybiomoleculesproteinsenzymes Palabras clave Amino acids organozinc reagents palladium peptides Programa(s) FP6-MOBILITY - Human resources and Mobility in the specific programme for research, technological development and demonstration "Structuring the European Research Area" under the Sixth Framework Programme 2002-2006 Tema(s) MOBILITY-2.1 - Marie Curie Intra-European Fellowships (EIF) Convocatoria de propuestas FP6-2002-MOBILITY-5 Consulte otros proyectos de esta convocatoria Régimen de financiación EIF - Marie Curie actions-Intra-European Fellowships Coordinador UNIVERSITY OF SHEFFIELD Aportación de la UE Sin datos Dirección Western Bank, firth court SHEFFIELD Reino Unido Ver en el mapa Coste total Sin datos
